1. OPA1: How much do we know to approach therapy?
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  2. Mitochondrial dysfunction caused by novel ATAD3A mutations
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  4. Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants
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  5. Mitochondrial Retinopathies
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  6. Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
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  7. Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
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  8. Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations
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  9. Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics
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  10. Leigh-like syndrome due to OPA1 mutations
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  11. High-glucose Induced Mitochondrial Dynamics Disorder of Spinal Cord Neurons in Diabetic Rats and its Effect on Mitochondrial Spatial Distribution
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  12. Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies
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  13. Systematic review of autosomal recessive ataxias and proposal for a classification
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  14. Mitochondrial disorders of the retinal ganglion cells and the optic nerve
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